The Analytical R&d Organization

Pharmaceutical

AssociateScientist,QC

$60–60k Andover, Massachusetts, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“Associate Scientist, QC at The Analytical R&d Organization. Skills: Quality Control, Analytical R&D, Biological therapeutics. Conduct qualitative and quantitative analyses. Verify identity, purity, and homogeneity”

Industry & Context.

Pharmaceutical
Problems you'll solve

Problem-solving skills

Eligibility Requirements

Wear PPE, Occasional light lifting, Periods of standing, Periods of sitting, Periods of walking, Occasional off-shift work

What They're Looking For.

Must Have

BAS with any years of experience, Experience in Quality Systems within a Good Manufacturing Practices (cGMP) environment, Proficiency with laboratory data systems, Hands-on experience or working knowledge in the pharmaceutical industry, Understanding of the drug development process, Excellent documentation skills, High attention to detail, Organizational abilities, Team-oriented mindset

Nice to Have

Hands-on analytical experience with biological therapeutics, Proficiency in operating analytical and physical techniques, Effective interpersonal skills, Ability to work collaboratively, Problem-solving skills, Experience with advanced analytical techniques, Knowledge of regulatory requirements, Ability to manage multiple tasks, Experience using common AI tools, Demonstrated curiosity for exploring AI tools, Understanding of responsible AI practices

What You'll Do.

Conduct qualitative and quantitative analyses

Prepare technical documents

Review technical documents

Analyze experimental data

Conduct experiments for analytical method development

Conduct experiments for analytical method qualification

Conduct experiments for analytical method validation

Conduct experiments for characterization

Complete Good Laboratory Practice training

Complete safety training

Adhere to departmental requirements

Maintain safety practices

How You'll Work.

Team & Collaboration

Group discussions

Full Job Description

**Use Your Power for Purpose** Pfizer’s purpose is to deliver breakthroughs that change patients’ lives. At the core of fulfilling this purpose is our commitment to Research and Development, where we strive to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are involved in discovery sciences, ensuring drug safety and efficacy, or supporting clinical trials, you will leverage cutting-edge design and process development capabilities to accelerate and deliver best-in-class medicines to patients globally. **What You Will Achieve** The qualified candidate will join the Analytical R&D organization in Andover, MA, to enable development of biological therapeutics. Within Analytical R&D the candidate will join the Quality Control – Andover Group focused on monoclonal antibodies/fusion proteins/synthetic peptides and other biological modalities. This group supports GMP analytical testing to progress biotherapeutic products in the pipeline; this includes release and stability testing, real time in-process testing support, and technical writing of reports and methods/procedure. **How You Will Achieve It** * Conduct qualitative and quantitative analyses of organic, inorganic compounds, or biologics. * Verify the identity, purity, and homogeneity of compounds during chemical syntheses, fermentation, or drug product development processes. * Prepare and review technical documents, including analytical test methods, standard operating procedures, and investigation reports. * Independently analyze experimental data and provide conclusions. * Follow procedures for assigned tasks; seek guidance when needed. * Conduct experiments for analytical method development, qualification, validation, and characterization of biological therapeutics. * Present problems and propose solutions in group discussions. * Complete all required Good Laboratory Practice and safety training, adhering to departmental requirements. * Maintain appropriate

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